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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847746Generated: October 30, 2026

3-Hydroxybenzaldehyde → 1-(3-Hydroxybenzyl)piperidine

https://huagongshe.com/reaction/847746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantPiperidineHCID 8082—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product1-(3-Hydroxybenzyl)piperidineHCID 82697474.5%

Reaction Steps

Piperidine (26 g) and 4.7 g of sodium borohydride were added to a solution of 15 g of 3-hydroxybenzaldehyde in 100 ml of ethanol, and the mixture was stirred until a complete solution formed. The solution was allowed to stand overnight at room temperature. Under reduced pressure, the solvent was distilled off, and 200 ml of ice water was added to the residue. The mixture was acidified with hydrochloric acid, and allowed to stand for 1 hour. The raw material was extracted away using ethyl acetate, and the aqueous solution was separated. The aqueous layer was alkalized with aqueous ammonia, and the precipitated oily product was extracted with ethyl acetate. The solvent was distilled off, and the residue was recrystallized from acetone/n-hexane to afford 17.5 g of 3-(1-piperidinylmethyl)phenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04293557
Source datasetuspto-grants-1981_10
ORD IDord-1ba48d1bcb0f4bfb829b23d2dc5cc2d0
Source noteuspto-grants-1981_10